A microfabricated 3-D stem cell delivery scaffold for retinal regenerative therapy

Thesis (M. Eng.)--Harvard-MIT Division of Health Sciences and Technology, 2009. === Cataloged from PDF version of thesis. === Includes bibliographical references (p. 59-61). === Diseases affecting the retina, such as Age-related Macular Degeneration (AMD) and Retinitis Pigmentosa (RP), result in the...

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Main Author: Sodha, Sonal
Other Authors: Sarah Tao and Robert Langer.
Format: Others
Language:English
Published: Massachusetts Institute of Technology 2010
Subjects:
Online Access:http://hdl.handle.net/1721.1/54593
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spelling ndltd-MIT-oai-dspace.mit.edu-1721.1-545932019-05-02T16:19:01Z A microfabricated 3-D stem cell delivery scaffold for retinal regenerative therapy Sodha, Sonal Sarah Tao and Robert Langer. Harvard University--MIT Division of Health Sciences and Technology. Harvard University--MIT Division of Health Sciences and Technology. Harvard University--MIT Division of Health Sciences and Technology. Thesis (M. Eng.)--Harvard-MIT Division of Health Sciences and Technology, 2009. Cataloged from PDF version of thesis. Includes bibliographical references (p. 59-61). Diseases affecting the retina, such as Age-related Macular Degeneration (AMD) and Retinitis Pigmentosa (RP), result in the degeneration of the photoreceptor cells and can ultimately lead to blindness in patients. There is currently no cure for AMD or RP, and only a few methods exist for slowing the progression of these diseases. Although there has been much recent headway in cell replacement therapy to restore vision loss, a number of challenges still remain. More specifically, there is a need for the development of a device that can deliver a large number of cells to the posterior segment of the eye, while promoting cell survival, differentiation and integration into the retina following transplantation. This research focuses on designing a device to meet these demands and improve the vision of those afflicted with blinding diseases. The specific hypothesis behind the proposed research is that a MEMS-based strategy to engineer a device can provide precisely defined spatial and chemical cues to influence retinal progenitor cells (RPCs) attachment, promote differentiation, and provide physical guidance in a more normal anatomical organization for their integration as neurosensory retina after transplantation to the subretinal space. Therefore, the specific aims of this research are to design, fabricate, and evaluate in vitro a novel ultrathin 3-D device made of polycaprolactone (PCL) for retinal cell replacement synthesized by the stacking, aligning, and bonding of three uniquely designed layers. (cont.)Photolithography, standard replica molding, and soft lithography techniques are used to fabricate the device elements. The 3-D device is designed with a defined cage structure to encapsulate a large number of cells. Another layer of the design allows for unidirectional cell migration out of one end into the subretinal space with the aid of contact guidance ridges. The third design layer allows for nutrient infiltration from the retinal pigment epithelium into the cell cages. The ultimate goal is to provide an environment compatible with the normal retinal tissue and conducive to the formation of functional synapses under the appropriate conditions, thereby restoring proper vision. With demonstration of efficacy and cell retention in vitro, the scaffold has the potential to reverse retinal degeneration due to disease or trauma and improve retinal function and integrity in vivo. by Sonal Sodha. M.Eng. 2010-04-28T17:06:31Z 2010-04-28T17:06:31Z 2009 2009 Thesis http://hdl.handle.net/1721.1/54593 586023451 eng M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission. http://dspace.mit.edu/handle/1721.1/7582 61 p. application/pdf Massachusetts Institute of Technology
collection NDLTD
language English
format Others
sources NDLTD
topic Harvard University--MIT Division of Health Sciences and Technology.
spellingShingle Harvard University--MIT Division of Health Sciences and Technology.
Sodha, Sonal
A microfabricated 3-D stem cell delivery scaffold for retinal regenerative therapy
description Thesis (M. Eng.)--Harvard-MIT Division of Health Sciences and Technology, 2009. === Cataloged from PDF version of thesis. === Includes bibliographical references (p. 59-61). === Diseases affecting the retina, such as Age-related Macular Degeneration (AMD) and Retinitis Pigmentosa (RP), result in the degeneration of the photoreceptor cells and can ultimately lead to blindness in patients. There is currently no cure for AMD or RP, and only a few methods exist for slowing the progression of these diseases. Although there has been much recent headway in cell replacement therapy to restore vision loss, a number of challenges still remain. More specifically, there is a need for the development of a device that can deliver a large number of cells to the posterior segment of the eye, while promoting cell survival, differentiation and integration into the retina following transplantation. This research focuses on designing a device to meet these demands and improve the vision of those afflicted with blinding diseases. The specific hypothesis behind the proposed research is that a MEMS-based strategy to engineer a device can provide precisely defined spatial and chemical cues to influence retinal progenitor cells (RPCs) attachment, promote differentiation, and provide physical guidance in a more normal anatomical organization for their integration as neurosensory retina after transplantation to the subretinal space. Therefore, the specific aims of this research are to design, fabricate, and evaluate in vitro a novel ultrathin 3-D device made of polycaprolactone (PCL) for retinal cell replacement synthesized by the stacking, aligning, and bonding of three uniquely designed layers. === (cont.)Photolithography, standard replica molding, and soft lithography techniques are used to fabricate the device elements. The 3-D device is designed with a defined cage structure to encapsulate a large number of cells. Another layer of the design allows for unidirectional cell migration out of one end into the subretinal space with the aid of contact guidance ridges. The third design layer allows for nutrient infiltration from the retinal pigment epithelium into the cell cages. The ultimate goal is to provide an environment compatible with the normal retinal tissue and conducive to the formation of functional synapses under the appropriate conditions, thereby restoring proper vision. With demonstration of efficacy and cell retention in vitro, the scaffold has the potential to reverse retinal degeneration due to disease or trauma and improve retinal function and integrity in vivo. === by Sonal Sodha. === M.Eng.
author2 Sarah Tao and Robert Langer.
author_facet Sarah Tao and Robert Langer.
Sodha, Sonal
author Sodha, Sonal
author_sort Sodha, Sonal
title A microfabricated 3-D stem cell delivery scaffold for retinal regenerative therapy
title_short A microfabricated 3-D stem cell delivery scaffold for retinal regenerative therapy
title_full A microfabricated 3-D stem cell delivery scaffold for retinal regenerative therapy
title_fullStr A microfabricated 3-D stem cell delivery scaffold for retinal regenerative therapy
title_full_unstemmed A microfabricated 3-D stem cell delivery scaffold for retinal regenerative therapy
title_sort microfabricated 3-d stem cell delivery scaffold for retinal regenerative therapy
publisher Massachusetts Institute of Technology
publishDate 2010
url http://hdl.handle.net/1721.1/54593
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